Genomic translocation breakpoint sequences are conserved in BCR-ABL1 cell lines despite the presence of amplification

Cancer Genetics and Cytogenetics

Volumn 189, Issue 2, 2009, Pages 138-139

  Ross, David M ^a   Schafranek, Lisa ^a   Hughes, Timothy P ^a   Nicola, Mario ^a   Branford, Susan ^a   Score, Joannah ^b  

^a INSTITUTE OF MEDICAL AND VETERINARY SCIENCE   (Australia)

^b WESSEX REGIONAL GENETICS LABORATORY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AGAROSE; BCR ABL PROTEIN; DNA; ETHIDIUM BROMIDE; GENOMIC DNA; MESSENGER RNA;

CHROMOSOMAL INSTABILITY; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; FUSION GENE; GENE AMPLIFICATION; GENE EXPRESSION; GENETIC CONSERVATION; HUMAN; LETTER; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION;

BASE SEQUENCE; CELL LINE, TUMOR; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 9; CONSERVED SEQUENCE; FUSION PROTEINS, BCR-ABL; GENE AMPLIFICATION; HUMANS; K562 CELLS; KARYOTYPING; TRANSLOCATION, GENETIC;

EID: 59749102355     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2008.10.010     Document Type: Letter

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